Biology:CMTX2

From HandWiki
Short description: Genetic element in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example


Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) is a protein that in humans is encoded by the CMTX2 gene.[1] Its cytogenetic location is Xp22.2.[2] It is associated with a variant of Charcot-Marie-Tooth disease.[1]

References

  1. ↑ 1.0 1.1 "Entrez Gene: Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)". https://www.ncbi.nlm.nih.gov/gene/1253. Retrieved 2014-02-23. 
  2. ↑ "CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 2; CMTX2". https://omim.org/entry/302801. 

Further reading



Retrieved from "https://handwiki.org/wiki/index.php?title=Biology:CMTX2&oldid=4095350"